Pili Expression Team

This team includes Marc Singer, Kevin Joseph, and Alena Wu.

6/28/2010

Made a 500 mL batch of LB broth

• When pouring in distilled water, pour a few mL at a time to avoid clumping.
• It takes 20g of powder to make 1 L of broth

Sterilized broth using the autoclave

• The temperature setting on the autoclave is off by a little bit
• Set dial 2 notches below 134°C.

6/29/2010

Started growing E. coli K12 cultures

• Poured 2 mL of LB broth into a Falcon tube
• Used strain of K12 from Dr. Lin's freezer
• Placed in incubator shaker for 24 hrs.

Added and inventoried supplies from Dr. Pinto's lab.

• Regular trash can be thrown out by going down one floor, then going outside to the trash bins.
• Chemical wastes must be cleaned by calling OSEH.

6/30/2010

Cryopreserved stock of K12

• 1 mL located in the iGEM box in the Lin lab.
• 1 mL located in the lab freezer.

7/1/2010

Cryopreserved DH5α according to protocol procedure on 6/30/2010

• Put 1 stock in -20°C fridge in 1239
• Put the other stock in the -80°C fridge in the Lin lab

7/7/2010

Obtain genomic DNA of CFT073 E. coli strain from Dr. Mobley's Lab

• stored in -20°C fridge on ice

7/21/2010

Kevin, Marc, Alena

Met in Dude to determine sequence of fim operon. Arranged meeting with Dr. Mobley's group next Tuesday to learn more about hyperpiliation and the cloning process.

7/27/2010

Kevin, Marc, Alena

Met with Chris Alteri from Dr. Harry Mobley's research group to discuss the best route to hyperproduce the pili. Chris recommended that we create a plasmid by cloning FimB into pBAD, and then inserting that plasmid in MG1655. In theory, that should activate flocculation in the E. coli, inducible by arabinose. Chris was able to give us the procedures for creating a plasmid with FimB, as well as the procedures for knocking out a gene.

In order to test how effectively the pili flocculate, we are planning to create an E. coli strain with fimE knocked out.

8/7/2010

Kevin, Marc, Alena

PCR #1 Used a gradient from 40C to 60C for the first 3 cycles to find the optimum anneling temperature.

All of the annealing temperatures gave a good result according to the gel.

8/7/10 notes

8/9/2010

Kevin, Marc, Alena

Used a 57C degree annealing temperature to get enough DNA for the digest and ligation.

4 out of the 5 PCR reactions worked well according to the gel.

The 5th well could have been a loading problem or there wasn't enough DNA.

8/9/10 notes

8/11/2010

Kevin, Marc

Met with Chris, received advice for updating digest and ligation protocols.

8/12/2010

Kevin, Marc, Alena

Met and discussed protocols for digestion and ligation of FIMB into pBAD.

1. Added 5 mL of LB broth each to 2 50 mL falcon tubes in the ERB lab using sterile technique.

2. Added 5 microliters of Kanamycin to each of the 50 mL tubes in step 1.

Went to the budget committee meeting for 1 hour with the tubes.

3. Obtained the cryostock of pBAD from the Lin -80C freezer (iGEM box cell #73)

4. Stabbed cryostock using a sterile 200 microliter pipette tip and pipetted into media from step 2.

5. At 8:05PM placed the two falcon tubes from step 4 into the incubator/shaker at 30C.

8/14/2010

Kevin, Marc, Alena

Miniprep pBAD plasmid

1. inoculate 5.0mL LB in 50mL conical tubes w/ 100ug/mL of ampilicin
   1. the cultures (2 of them) grew for ~12hrs (8am to 8pm)
2. centrifuge (using the 50mL conical tubes) for 5000rpm for 10min at 4C
3. carefully discard the supernatant and resuspend the pellet with 250uL of P1 buffer (kept in the 4C fridge)
4. transfer into a labelled 1.5mL eppendorf tube (set pipetman to 500uL just in case)
5. add 250uL P2 Buffer--> invert 4-6times (should turn blue)--> add 350uL N3 buffer--> invert 4-6times (should become vicious or clumpy)
   1. centrifuge for 13,000rpm for 10mins
6. pipet out supernatant into a QIA spin column--> centrifuge for 60s--> discard flow through
   1. did not pipet out all of the supernatant
7. add 500uL PB buffer --> centrifuge 60s--> discard flow through
8. add 750uL PE buffer--> centrifuge 60s--> discard--> centrifuge 60s again
9. transfer into a labeled 1.5mL eppendorf tube--> add 50uL EB (elution buffer)
   1. allow it to sit for 1 min (it helps to release the DNA from the column)

fimB PCR product Purification

1. Used sample A and B of PCR product (save C and D for later)
   1. total volume of PCR product = 81 uL (40.5uL separately)
2. add 5 volumes of PB buffer (202.5uL) to 1 volume of PCR product (40.5uL); invert
3. transfer into a QIAquick spin column (provided in the Qiagen kit)
   1. set pipetman to 260uL to be sure to get all of the mixture
4. centrifuge spin column at 13,000rpm for 60s
5. discard the flow through (in the collection tube) and add 750uL PE buffer (to wash the DNA)

repeat step 4 again

1. discard flow through and centrifuge again to get the remain buffers out
2. place the column into a labeled 1.5mL eppendorf tube
3. add 50uL EB buffer (to elute out the DNA) directly to the white inner circle of the column (avoid touching the pipet tip to the column)
   1. allow the mix to sit in the column for 1 min, then centrifuge for 1 min (13,000rpm)
   2. remember to point the cap of the eppendorf tube in the opposite direction of the centrifuge machine

fimB Digest

1. pre-programmed PCR machine to Digest (DIG1)
2. use 5 PCR reaction tubes for each; 5 for fimB and 5 for pBAD
3. add the following amounts in that order (total volume of 20uL)

• 16 uL of the DNA (fimB and pBAD to their respective tubes)
• 2 uL of NEB 2 buffer
• 1 uL NcoI
• 1uL HindIII

1. incubate for 37C overnight (12hrs)
   1. place into 4C fridge the next day

8/16/2010

Kevin, Marc, Alena

Alena order/picks up NEB Ligase (T4 DNA Ligase, 20,000U/mL) from MSRB II enzyme store

Attempted experiment:

• Added 1uL of CIP (Calf Intestine Phosphatase) to plasmid reactions only (pBAD)
  • CIP will cut off the 3' phosphate to prevent the plasmid from folding back on itself
• incubate CIP-pBAD at 37C for 1 hr and then heat-shock (65C for 15 min)

We made a huge human error when setting up our thermal cycle program on the PCR machine. We did not realize we only set the thermal cycle for our digest on [1] for 12 minutes (12:00) rather than the intended time period of 12 hours (12:00:00). This explains the condensation present in the PCR machine (it stayed at 4C for too long). We discovered our mistake after running the incubation of CIP+pBAD for 37C for (1:00) 1 minute then heat-shock at 65C for 15 minute. It is VERY IMPORTANT to triple check one another when entering in any program.

Rest of the day:

• headed over to the ERB and made two cultures of 5mL LB-Amp (in 50mL conical tubes)--> placed in the Lin Lab 4C fridge

In the Lab